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- NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_assertion type Assertion NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_head.
- NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_assertion description "[Epidermolytic ichthyosis (EI) is a hereditary keratinization disorder caused by mutations in the keratin 1 (KRT1) or keratin 10 (KRT10) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_provenance.
- NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_assertion evidence source_evidence_literature NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_provenance.
- NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_assertion SIO_000772 21271994 NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_provenance.
- NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_assertion wasDerivedFrom befree-2016 NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_provenance.
- NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_assertion wasGeneratedBy ECO_0000203 NP868178.RAA3Hp5wvMJBkz07tasK6xPWbavDjdrv_SqVvb2C2zN7M130_provenance.